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Aversive emotional tension of anorectic patients in daily course: A controlled and smartphone-based ambulatory monitoring

Aversive emotional tension of anorectic patients in daily course: A controlled and smartphone-based ambulatory monitoring - SMART

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00005228
Enrollment
40
Registered
2013-09-02
Start date
2013-09-03
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

F50.0

Interventions

Group 1: patient group: Female patients with F50.0 diagnosis will be questioned hourly for 2 days on their own smartphones about their experienced emotional tension. Group 2: control group: Mentally

Sponsors

Klinik und Poliklinik für Kinder- und Jugendpsychiatrie und -psychotherapie der Universitätsmedizin Mainz
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
12 Years to 19 Years

Inclusion criteria

Inclusion criteria: informed consent of subject and parents patient group: current diagnosis of an eating disorder F50.0

Exclusion criteria

Exclusion criteria: patient group: (Presumed) diagnosis of an emotional instable personality disorder F60.31 (borderline) or F60.30 (impulsive). control group: any diagnosis of a mental disorder in the last 5 years

Design outcomes

Primary

MeasureTime frame
mean value of emotional tension (single values measured hourly in the ambulatory monitoring over 2 days)

Secondary

MeasureTime frame
Maximum value of emotional tension, course of emotional tension, emotion recognition rate (single values measured hourly in the ambulatory monitoring over 2 days), compliance (missing values).

Countries

Germany

Contacts

Public ContactDavid Kolar

Universität Regensburg

David.Kolar@psychologie.uni-regensburg.de0941 943-7551

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 13, 2026